Clearance Summary
PBI MULTILASE D COPPER VAPOR LASER received FDA 510(k) clearance under submission number K920004, sponsored by Wm.I.Kern & Co., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1992-05-14.
- Submission: K920004
- Applicant / Sponsor: Wm.I.Kern & Co., Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 1992-05-14
Classification & Regulation
This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.